Clinical Study Manager
I
ICONMA, LLC
📍 United States, United States, United States
Job Description
Our client, a Pharmaceutical company, is looking for a Clinical Study Manager for their Durham, NC location. Responsibilities:
+ The Contract Clinical Study Manager provides operational leadership, coordination, and oversight for assigned clinical studies. This role supports the successful execution of study activities in accordance with ICH/GCP guidelines, applicable regulatory requirements, company SOPs, study protocols, and study-specific plans. The Contract Clinical Study Manager works closely with internal cross-functional teams, CROs, vendors, investigators, and study site personnel to ensure study deliverables are completed with quality, within expected timelines, and in alignment with study objectives.
+ Provide day-to-day study management support and oversight for assigned clinical study activities from start-up through close-out.
+ Coordinate with internal project team members, CROs, vendors, investigators, and study coordinators to support ...
+ The Contract Clinical Study Manager provides operational leadership, coordination, and oversight for assigned clinical studies. This role supports the successful execution of study activities in accordance with ICH/GCP guidelines, applicable regulatory requirements, company SOPs, study protocols, and study-specific plans. The Contract Clinical Study Manager works closely with internal cross-functional teams, CROs, vendors, investigators, and study site personnel to ensure study deliverables are completed with quality, within expected timelines, and in alignment with study objectives.
+ Provide day-to-day study management support and oversight for assigned clinical study activities from start-up through close-out.
+ Coordinate with internal project team members, CROs, vendors, investigators, and study coordinators to support ...